Identification of c.104T>G, p.Met35Arg (NM_00314.8) heterozygous variant in exon 2 of PTEN as the causative factor for Cowden syndrome: a medical case study
- Mansilla-Polo, M.
- Escutia-Muñoz, B.
- Llavador-Ros, M.
- Botella-Estrada, R.
ISSN: 1365-2230
Year of publication: 2024
Volume: 49
Issue: 2
Pages: 203-205
Type: Article